Analyze Your Search

Hints:

  • Action links for each search result record
    • Bookmark: Allows you to Bookmark the page for easy future retrieval 
    • Email: Opens a pop-up window where you can write a message to the recipient of the email
    • Copy URL: Copies the URL of the requested document for pasting in an email or other document
    • More Info: Shows full summary of content record
  • Saved Searches and Alerts
    • Save your search for later viewing & updates by clicking the blue "Follow" button to the right of the search box. 
Antenatal/Prenatal Care
  Follow Topic   Edit Search
Your search returned 22 results
from the time period: last 30 days.
Sort by Relevance / Date Group By Journal / No Grouping
Prenatal diagnosis
AbstractText: To explore parental experiences of whole exome sequencing (WES) for prenatal diagnosis and ascertain what influenced their decision-making to undergo testing AbstractText: Twelve women comprised a purposeful sample in a series of semistructured interviews. All had received a fetal anomaly diagnosis on ultrasound. A topic guide was used, and transcripts were thematically analyzed to elicit key themes AbstractText ...
Prenatal diagnosis
AbstractText: To investigate the significance of prenatal diagnosis of subependymal cysts (SEC... and confirmed by fetal brain Magnetic Resonance Imaging (MRI) AbstractText: We reviewed all the cases of isolated SEC diagnosed antenatally in our center from January 1(st) , 2014 to December 31(st) , 2015 and confirmed by fetal MRI ...
Cysts (2), more mentions
American journal of obstetrics and gynecology
... plus additional structural anomalies (48.9% vs. 14.3%, P < 0.0001) or intrauterine growth retardation group (50.0% vs. 14.3%, P = 0.044) was significantly higher than ... disease with additional structural anomalies and congenital heart disease with intrauterine growth retardation groups (48.9% vs. 50.0%), congenital heart disease with soft markers and congenital heart disease with intrauterine growth retardation groups (19.8% vs. 50.0%), as well as congenital heart disease ...
Cardiovascular Diseases (17)
Heart Diseases (17), Fetal Growth Retardation (3), Chromosomal Duplication (1), more mentions
The Cochrane database of systematic reviews 
... Pregnancy and Childbirth's Trials Register, ClinicalTrials.gov, the WHO International Clinical Trials Registry Platform (ICTRP) (all searched 11 August 2017), and reference lists of retrieved studies AbstractText: Randomised and quasi-randomised trials (including those published in abstract form) comparing the effects of described antenatal ultrasound surveillance regimens in twin pregnancies.
Premature Birth (2), Acidosis (1), more mentions
BJOG : an international journal of obstetrics and gynaecology
... screened high risk were asked to decide among 1) an invasive test plus chromosomal microarray (CMA) to obtain more detailed fetal genetic information, 2) a non-invasive cell free prenatal DNA screening (NIPT) to detect trisomies 13, 18 and 21 to avoid procedure related miscarriage, and 3) decline further testing.
Down Syndrome (3), Spontaneous Abortion (2), Aneuploidy (1), more mentions
Prenatal diagnosis
... and explore the associated diagnostic and counseling challenges AbstractText: Cases were derived from a cohort of pregnant women who attended a multi-site specialist prenatal screening and ultrasound service for non-invasive prenatal testing by cell-free DNA analysis and mid-trimester fetal morphology assessment AbstractText: Seven cases of genotype ...
Delayed Puberty (1), Infertility (1), more mentions
The Cochrane database of systematic reviews 
Prenatal screening for fetal aneuploidies is standard care in many countries, but ... reference lists of relevant full-text articles, websites of private prenatal diagnosis companies and conference abstracts AbstractText: Studies could include pregnant women ... The accuracy of gNIPT as a prenatal screening test has been mainly evaluated as a second-tier screening ...
Aneuploidy (7), Trisomy (2), Down Syndrome (2), more mentions
Prenatal diagnosis
Prenatal diagnosis of Chronic Intestinal Pseudo-Obstruction and paternal somatic mosaicism for the ACTG2 pathogenic variant..
Intestinal Pseudo-Obstruction (2), more mentions
Prenatal diagnosis
Comment on "Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome"..
Prenatal diagnosis
Comment on "The clinical utility of genome-wide non invasive prenatal screening"..
Prenatal diagnosis
... impact of offering cfDNA screening as a first tier test for trisomies 21 and 18 AbstractText: This is a prospective study of pregnant women undergoing conventional prenatal screening who were offered cfDNA screening in the first trimester with clinical outcomes obtained on all pregnancies AbstractText: 1198 pregnant women were recruited.
Trisomy (2), Down Syndrome (1), more mentions
The Journal of emergency medicine
AbstractText: Ectopic pregnancy (EP) is an important cause of morbidity and mortality in females of reproductive age. Proper diagnosis and treatment are critical, as complications such as rupture, hemorrhagic shock, and even death can occur AbstractText: EP is a condition emergency physicians are trained to detect, yet there are multiple myths concerning its evaluation and diagnosis.
Men's Health (3)
Ectopic Pregnancy (2), Hemorrhagic Shock (1), more mentions
European journal of pediatrics
Nowadays, CPAM are diagnosed prenatally, improving the prenatal and immediate postnatal care and ultimately the knowledge on CPAM pathophysiology... Congenital pulmonary airway malformations (CPAM) are rare developmental lung malformations mainly antenatally diagnosed. While the neonatal management of symptomatic CPAM is clear and includes prompt surgery, controversies remain for asymptomatic CPAM due to risk of infections and malignancies.
Infections (4), Pulmonary Blastoma (1), more mentions
Archives of disease in childhood 
... education and routine penicillin prophylaxis AbstractText: Age seen by a specialist clinician, age at prescription of penicillin prophylaxis and mortality AbstractText: All but two resident cases of SCD were identified through screening; one baby was enrolled in care after prenatal diagnosis; one baby whose parents refused newborn screening presented symptomatically.
Infectious Diseases (1), Vaccines (1)
Sickle Cell Anemia (1), more mentions
Journal of pediatric surgery
... itself, accounts for the reported poorer survival in right-sided CDH AbstractText: Level I for a prognosis study - This is a high-quality, prospective cohort study with 99% of patients followed to the study end point (death or discharge) Keyword: Congenital diaphragmatic hernia (CDH. Keyword: Defect side. Keyword: Defect size. Keyword: Extracorporeal membrane oxygenation (ECMO. Keyword: Prenatal diagnosis. Keyword: Survival.
Hernia (3), more mentions
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
Countries were classified by World Health Organization regions. Sensitivity analyses were conducted AbstractText: The database included 1103 prevalence measures from 136 million syphilis tests across 154 countries (85% from antenatal care women. Global pooled mean prevalence (weighted by region population size) was 1.11% (95% confidence interval [CI]: 0.99-1.22. Prevalence predictors were region, diagnostic assay, sample size, and calendar year ...
Syphilis (6), Infections (1), more mentions
European journal of pediatrics
Congenital heart disease is regarded to be the most important clinical phenomenon in children with Down syndrome, due to its significant impact on morbidity and mortality. New developments in prenatal diagnostic and therapy management of congenital heart disease continue to influence the number of patients diagnosed with congenital heart disease and Down syndrome. What is New.
Cardiovascular Diseases (8)
Down Syndrome (12), Heart Diseases (8), Congenital Heart Defects (1), more mentions
American journal of medical genetics. Part A
... 21; sometimes this rearrangement may also lead to segmental monosomy of the terminal long arm of chromosome 21. In this report, we describe the prenatal diagnosis and neonatal follow-up of a child with a paternally derived, de novo isodicentric chromosome 21 and a concurrent ∼1.2 Mb deletion of the 21q22.3 region [46,XX,idic(21)(q22.3... Keyword: prenatal diagnosis.
Down Syndrome (4), Monosomy (3), Tethered Cord Syndrome (1), more mentions
The Journal of clinical endocrinology and metabolism
A single-blind randomized clinical trial was undertaken on SCH-TPOAb- pregnant women AbstractText: Prenatal care centers of Shahid Beheshti University of Medical Sciences AbstractText: Using the thyrotropin (TSH) cut-point of 2.5mIU/L, 366 SCH-TPOAb- and 1092 euthyroid TPOAb- women were recruited AbstractText: SCH-TPOAb- women were randomly ...
Hypothyroidism (1), more mentions
Contraception
To describe women's pain during the procedure, we recruited women during antenatal care and at the time of admission for delivery until we collected at least 30 sets of pain scores at two time points (pre-procedure and immediately post-procedure) in both groups using two instruments; 100mm visual analogue ...
Women's Health (3)
Labor Pain (1), more mentions
1 2  | Next Page»